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The Role of Iodinated Compounds and Molecular Iodine in Human Disease

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Biochemistry".

Deadline for manuscript submissions: 20 October 2025 | Viewed by 445

Special Issue Editor


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Guest Editor
Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Juriquilla 76230, Querétaro, Mexico
Interests: molecular iodine; cancer biology; cancer biomarkers

Special Issue Information

Dear Colleagues,

Iodine, in its various chemical forms, is essential for most living organisms and considered a micronutrient in chordates. In vertebrates, iodine is a vital component of thyroid hormones, crucial for the proper development and functioning of several organs, particularly in the nervous system. However, a significant amount of iodine in the body is non-hormonal and concentrated in extra-thyroid tissues, where its biological function is not well understood. Some scientific groups have suggested that iodine may have an outdated antioxidant function in all the cells that concentrate it, from primitive algae to recent vertebrates. In these cells, oxidized iodine can act as an electron donor, neutralizing reactive oxygen species (ROS), or attach to the double bonds of certain polyunsaturated fatty acids in cell membranes, making them less reactive to ROS. Additionally, it has been demonstrated that iodine binds to lipids, such as arachidonic acid, induces apoptosis, and has differentiation effects on various cancer cells. Furthermore, iodine is taken up and metabolized by immune cells, and depending on the physiological context, this halogen can act as an anti-inflammatory or pro-inflammatory agent.

Recently, the I2 supplement prevented and normalized metabolic alterations in a diabetic mouse model induced with streptozotocin, preserving the morphology of pancreatic, liver, muscle, and adipose tissues and promoting the abundance of beneficial bacteria that support the integrity of the intestinal epithelial barrier and higher α-diversity. This Special Issue aims to provide an overview of “The Role of Iodinated Compounds and Molecular Iodine in Human Disease” and their potential applications.

Dr. Carmen Aceves
Guest Editor

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Keywords

  • iodine
  • iodinated compounds
  • oxidized iodine
  • oxidized iodine supplement

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Published Papers (1 paper)

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Research

16 pages, 12668 KiB  
Article
Molecular Iodine Exhibited Differential Antiproliferative Actions in Progenitor and Stem Populations from Chemoresistant Cancer Cells
by Irasema Mendieta, Jazmin Leon-Pichardo, Gustavo Orizaga-Osti, Edgar R. Juvera-Avalos, Uriel Rangel-Chavez, Evangelina Delgado-Gonzalez, Brenda Anguiano and Carmen Aceves
Int. J. Mol. Sci. 2025, 26(9), 4020; https://doi.org/10.3390/ijms26094020 - 24 Apr 2025
Viewed by 169
Abstract
Cancer stem cells (CSCs) are described as a subpopulation of cells with capabilities of self-renewal, chemoresistance, and invasiveness. CSCs reside in tumor niches and can be studied in vitro through their enrichment in spheroids (Stem). Molecular iodine (I2) induces apoptosis and [...] Read more.
Cancer stem cells (CSCs) are described as a subpopulation of cells with capabilities of self-renewal, chemoresistance, and invasiveness. CSCs reside in tumor niches and can be studied in vitro through their enrichment in spheroids (Stem). Molecular iodine (I2) induces apoptosis and differentiation in various cancer cells. I2 can activate peroxisome proliferator-activated receptors type gamma (PPARγ), and its pathways are associated with its oxidant/antioxidant capacity. This work aimed to compare the effect of I2 supplementation in progenitor and CSC populations with low (MCF-7 and S-K-NAS) and high invasiveness (MDA-MB231 and SK-N-BE2) in mammary and neuroblastoma (NB) cell lines. Results showed that the CSC population enriched by the spheroid culture overexpressed stem messengers CD44, SOX2, and NMYC and exhibited the highest mitochondrial metabolism (membrane mitochondrial potential and O2). The presence of I2 increases PPARγ expression and induces apoptosis through the Bax/Bcl2 index in all populations but silences NMYC expression and reduces mitochondrial metabolism in Stem NB. I2 also enhances the expression of nuclear erythroid factor 2 (Nrf2) in all populations, but the target antioxidant superoxide dismutase 2 (SOD2) is only elevated in progenitor cells. In contrast, the mitophagy inductors PTEN-induced putative kinase 1 (Pink1) and microtubule-associated protein1 light chain3 alpha (LC3) were overexpressed in Stem populations. I2-preselected SK-N-BE2 populations exhibited minor implantation and invasion capacities in the in vivo zebrafish model. These data indicate that I2 interferes with viability, implantation, and invasion capacity in all cell lines, but the molecular mechanisms vary depending on the progenitor or Stem condition. Full article
(This article belongs to the Special Issue The Role of Iodinated Compounds and Molecular Iodine in Human Disease)
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